jsp, welcome aboard!
Yours is a nice project, any chance to see the antherozoids under the microscope?
To get good illumination without that nasty specular reflections you have two posible approaches:
- Highly difussed illumination: surround the sample with a difusser material and place the light sources at some distance of it, the goal is to have a big surface uniformely illuminatig the sample from almost all directions. many materials can work, from dedicated light difussing materials to yogurt pots, kleenex tissues, half cutted pingpong balls... there are a lot of posts at the forum about, just seach for diffuser
- Cross polarized incident illumination, much less popular, but IMO it works very well for highly reflective fern cells, take a look to my old posts:
http://www.photomacrography.net/forum/v ... 7184#67184
http://www.photomacrography.net/forum/v ... 6730#56730
About light source both electronic flash and continous illumination may work very well. A single flash unit may be enough to illuminate a difuser, no real need to buy the expensive MT24.
For continuos illumination you don't need a powerfull source, a pair of inexpensive Ikea Janksjö LED lamps are very popular in forum members, a fiber optic illuminator would be even better.
Continous light is more flexible to set up the sample and illumination, set your 5DII at silent mode I ( EFSC) to avoid camera induced vibration blur .
To get the full gametophyte in focus you'll need for sure to use focus stacking techniques.
Another approach could be to place the sample under the microscope and do stack and stich wit a low power objective, what are the gametophyte dimensions?
Ans please ask any other more specific questions and clarifications.